Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting.
about
ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome.Elongation of the Kcnq1ot1 transcript is required for genomic imprinting of neighboring genesComparative sequence and x-inactivation analyses of a domain of escape in human xp11.2 and the conserved segment in mouseBidirectional action of the Igf2r imprint control element on upstream and downstream imprinted genesThe Tnfrh1 (Tnfrsf23) gene is weakly imprinted in several organs and expressed at the trophoblast-decidua interfaceUnbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11Identification of a new murine tumor necrosis factor receptor locus that contains two novel murine receptors for tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)Role of histone methyltransferase G9a in CpG methylation of the Prader-Willi syndrome imprinting center.Antisense transcripts with FANTOM2 clone set and their implications for gene regulation.Clusters of internally primed transcripts reveal novel long noncoding RNAs.Evolution of the CDKN1C-KCNQ1 imprinted domain.Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome.Allelic skewing of DNA methylation is widespread across the genome.Short interspersed transposable elements (SINEs) are excluded from imprinted regions in the human genome.Genome-wide survey reveals dynamic widespread tissue-specific changes in DNA methylation during development.Loss of CpG methylation is strongly correlated with loss of histone H3 lysine 9 methylation at DMR-LIT1 in patients with Beckwith-Wiedemann syndrome.ncRNAimprint: a comprehensive database of mammalian imprinted noncoding RNAs.Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes.Co-evolution of X-chromosome inactivation and imprinting in mammals.BACs as tools for the study of genomic imprinting.Imprinting disruption of the CDKN1C/KCNQ1OT1 domain: the molecular mechanisms causing Beckwith-Wiedemann syndrome and cancer.Extra-embryonic-specific imprinted expression is restricted to defined lineages in the post-implantation embryo.Chromosome-wide identification of novel imprinted genes using microarrays and uniparental disomies.Identification of novel imprinted genes in a genome-wide screen for maternal methylation.Regulation of supply and demand for maternal nutrients in mammals by imprinted genes.Chromosome-wide analysis of parental allele-specific chromatin and DNA methylation.Enhancers compete with a long non-coding RNA for regulation of the Kcnq1 domainThe silence RNA keeps: cis mechanisms of RNA mediated epigenetic silencing in mammals.Specific differentially methylated domain sequences direct the maintenance of methylation at imprinted genes.Depletion of Kcnq1ot1 non-coding RNA does not affect imprinting maintenance in stem cells.Imprinted silencing of Slc22a2 and Slc22a3 does not need transcriptional overlap between Igf2r and Air.The potential role of gene duplications in the evolution of imprinting mechanisms.Epigenetic asymmetry in the mammalian zygote and early embryo: relationship to lineage commitment?A survey for novel imprinted genes in the mouse placenta by mRNA-seqMIRA-SNuPE, a quantitative, multiplex method for measuring allele-specific DNA methylation.Dual Functions of the RFTS Domain of Dnmt1 in Replication-Coupled DNA Methylation and in Protection of the Genome from Aberrant Methylation.Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control regionAllele-specific binding of CTCF to the multipartite imprinting control region KvDMR1Comparative analysis of sequence characteristics of imprinted genes in human, mouse, and cattle.The influence of non-coding RNAs on allele-specific gene expression in mammals.
P2860
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P2860
Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting.
description
2000 nî lūn-bûn
@nan
2000 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Sequence and functional compar ...... entre and extended imprinting.
@ast
Sequence and functional compar ...... entre and extended imprinting.
@en
type
label
Sequence and functional compar ...... entre and extended imprinting.
@ast
Sequence and functional compar ...... entre and extended imprinting.
@en
prefLabel
Sequence and functional compar ...... entre and extended imprinting.
@ast
Sequence and functional compar ...... entre and extended imprinting.
@en
P2093
P356
P1476
Sequence and functional compar ...... entre and extended imprinting.
@en
P2093
Engemann S
Reinhardt R
Strödicke M
P304
P356
10.1093/HMG/9.18.2691
P50
P577
2000-11-01T00:00:00Z